{"title":"从结晶动力学的角度揭示磷回收过程中均匀结晶的关键控制因素","authors":"Xiang Li, Xin Hu, Shuting Shen, Rui Wan, Hongliang Dai, Xiwu Lu","doi":"10.1016/j.jclepro.2025.144782","DOIUrl":null,"url":null,"abstract":"Phosphorus (P) recovery from wastewater is a critical process for addressing environmental concerns associated with P pollution and promoting resource sustainability through the closure of the P cycle. However, the efficiency of P recovery is often hindered by homogeneous crystallization. This study aims to elucidate the role of homogeneous crystallization in hydroxyapatite (HAP) formation and its influence on P recovery efficiency. We employed pH monitoring to assess the induction time for homogeneous crystallization, while simultaneously tracking changes in calcium and P concentrations during both formation and transformation stages. Our findings indicate that adjusting operational parameters significantly influences P removal efficiency and the induction time for phase transition in the crystallization process. Specifically, increasing the pH from 8 to 10 resulted in an enhancement of P removal efficiency, rising from 36 % to 99 %. However, this increase in pH corresponded with a substantial prolongation of the induction time for phase transition, extending from 0.53 h to 15.8 h. In contrast, raising the temperature from 15 °C to 35 °C improved P removal efficiency from 23.62 % to 56.80 % while concurrently decreasing the induction time for phase transition from 10.45 h to 1.31 h. The transformation to HAP occurs primarily through the dissolution-recrystallization of ACP. By carefully regulating operational parameters, we can control the formation and transformation of the homogeneous precipitate, thereby enhancing P recovery efficiency. This research provides valuable insights into the composition, formation, and transformation mechanisms of fine particles during P recovery, while also offering a novel perspective for assessing the risks associated with homogeneous precipitates.","PeriodicalId":349,"journal":{"name":"Journal of Cleaner Production","volume":"55 1","pages":""},"PeriodicalIF":9.7000,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unravelling key factors controlling homogeneous crystallization during phosphorus recovery: From the perspective of crystallization kinetics\",\"authors\":\"Xiang Li, Xin Hu, Shuting Shen, Rui Wan, Hongliang Dai, Xiwu Lu\",\"doi\":\"10.1016/j.jclepro.2025.144782\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Phosphorus (P) recovery from wastewater is a critical process for addressing environmental concerns associated with P pollution and promoting resource sustainability through the closure of the P cycle. However, the efficiency of P recovery is often hindered by homogeneous crystallization. This study aims to elucidate the role of homogeneous crystallization in hydroxyapatite (HAP) formation and its influence on P recovery efficiency. We employed pH monitoring to assess the induction time for homogeneous crystallization, while simultaneously tracking changes in calcium and P concentrations during both formation and transformation stages. Our findings indicate that adjusting operational parameters significantly influences P removal efficiency and the induction time for phase transition in the crystallization process. Specifically, increasing the pH from 8 to 10 resulted in an enhancement of P removal efficiency, rising from 36 % to 99 %. However, this increase in pH corresponded with a substantial prolongation of the induction time for phase transition, extending from 0.53 h to 15.8 h. In contrast, raising the temperature from 15 °C to 35 °C improved P removal efficiency from 23.62 % to 56.80 % while concurrently decreasing the induction time for phase transition from 10.45 h to 1.31 h. The transformation to HAP occurs primarily through the dissolution-recrystallization of ACP. By carefully regulating operational parameters, we can control the formation and transformation of the homogeneous precipitate, thereby enhancing P recovery efficiency. This research provides valuable insights into the composition, formation, and transformation mechanisms of fine particles during P recovery, while also offering a novel perspective for assessing the risks associated with homogeneous precipitates.\",\"PeriodicalId\":349,\"journal\":{\"name\":\"Journal of Cleaner Production\",\"volume\":\"55 1\",\"pages\":\"\"},\"PeriodicalIF\":9.7000,\"publicationDate\":\"2025-01-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Cleaner Production\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jclepro.2025.144782\",\"RegionNum\":1,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, ENVIRONMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cleaner Production","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1016/j.jclepro.2025.144782","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
Unravelling key factors controlling homogeneous crystallization during phosphorus recovery: From the perspective of crystallization kinetics
Phosphorus (P) recovery from wastewater is a critical process for addressing environmental concerns associated with P pollution and promoting resource sustainability through the closure of the P cycle. However, the efficiency of P recovery is often hindered by homogeneous crystallization. This study aims to elucidate the role of homogeneous crystallization in hydroxyapatite (HAP) formation and its influence on P recovery efficiency. We employed pH monitoring to assess the induction time for homogeneous crystallization, while simultaneously tracking changes in calcium and P concentrations during both formation and transformation stages. Our findings indicate that adjusting operational parameters significantly influences P removal efficiency and the induction time for phase transition in the crystallization process. Specifically, increasing the pH from 8 to 10 resulted in an enhancement of P removal efficiency, rising from 36 % to 99 %. However, this increase in pH corresponded with a substantial prolongation of the induction time for phase transition, extending from 0.53 h to 15.8 h. In contrast, raising the temperature from 15 °C to 35 °C improved P removal efficiency from 23.62 % to 56.80 % while concurrently decreasing the induction time for phase transition from 10.45 h to 1.31 h. The transformation to HAP occurs primarily through the dissolution-recrystallization of ACP. By carefully regulating operational parameters, we can control the formation and transformation of the homogeneous precipitate, thereby enhancing P recovery efficiency. This research provides valuable insights into the composition, formation, and transformation mechanisms of fine particles during P recovery, while also offering a novel perspective for assessing the risks associated with homogeneous precipitates.
期刊介绍:
The Journal of Cleaner Production is an international, transdisciplinary journal that addresses and discusses theoretical and practical Cleaner Production, Environmental, and Sustainability issues. It aims to help societies become more sustainable by focusing on the concept of 'Cleaner Production', which aims at preventing waste production and increasing efficiencies in energy, water, resources, and human capital use. The journal serves as a platform for corporations, governments, education institutions, regions, and societies to engage in discussions and research related to Cleaner Production, environmental, and sustainability practices.